# Oakfield Instruments, Ltd.

- Location (FDA's records): Oxon Ox8 1ja   England, GB
- FDA decisions: 8 (1989–1997): 8 510(k) clearances
- Product codes: KLA (3), IZD (2), FFT (2), JJJ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K964804: Flexilog LS (Aug 6, 1997)
- K964589: Flexilog 3000 (Mar 4, 1997)
- K961895: Flexilog LS 13921 (Nov 4, 1996)
- K945069: Flexilog 2000 (Jun 13, 1995)
- K920115: Mediscint (Mar 30, 1992)
- K902460: Cardioscint (Left Ventricular Function Monitor) (Aug 28, 1990)
- K896288: Flexilog 1010 Ambulatory PH Monitoring System (May 4, 1990)
- K894902: Sourcerer (Oct 17, 1989)

Source page: https://510kreport.com/company/oakfield-instruments